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Philips FM20/30 Instructions For Use Manual Page 286

Release j.3 with software revision j.3x.xx patient monitoring.
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28 Specifications and Standards Compliance
Table 1 - Guidance and Manufacturer's Declaration: Electromagnetic Emissions
Emissions Test
RF emissions CISPR 11
For the Avalon FM40/FM50 with all
accessories.
For the Avalon FM20/30 fetal monitor
whenever used with the IUP/ECG patient
module M2738A.
For the Avalon CTS Interface Cable (M2731-
60001/M2732-60001) whenever used with the
Avalon CTS Cableless Fetal Transducer System.
For the Avalon CL Base Station with cableless
transducers whenever used with the fetal
monitors.
1
Note that the device is not intended for home use.
Electromagnetic Immunity
The monitor is suitable for use in the specified electromagnetic environment. The user must ensure
that it is used in the appropriate environment as described below.
Table 2 - Guidance and Manufacturer's Declaration: Electromagnetic Immunity
Immunity Test
Electrostatic discharge
(ESD)
IEC 61000-4-2
Electrical fast transient/
burst
IEC 61000-4-4
Surge
IEC 61000-4-5
286
Compliance
Class A
IEC 60601-1-2
Compliance Level
Test Level
±6 kV contact
±6 kV contact
±8 kV air
±8 kV air
±2 kV for power
±2 kV for power supply
supply lines
lines
±1 kV for input/
±1 kV for input/output
output lines
lines
±1 kV differential
±1 kV differential mode
mode
±2 kV common mode
±2 kV common
mode
Avoiding Electromagnetic Interference
The device is suitable for use in all
establishments other than domestic
establishments and those directly connected to
the public low-voltage supply network that
supplies buildings used for domestic purposes.
Electromagnetic Environment
Guidance
Floors should be wood, concrete, or
ceramic tile. If floors are covered with
synthetic material, the relative humidity
should be at least 30%.
Mains power quality should be that of a
typical commercial and/or hospital
environment
Mains power quality should be that of a
typical commercial and/or hospital
environment

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Avalon clFm40/50

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